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Ceria Nanoparticles Synthesized With Aminocaproic Acid for the Treatment of Subarachnoid Hemorrhage

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dc.contributor.authorJeong, Han-Gil-
dc.contributor.authorCha, Bong Geun-
dc.contributor.authorKang, Dong-Wan-
dc.contributor.authorKim, Do Yeon-
dc.contributor.authorKi, Seul Ki-
dc.contributor.authorKim, Song I.-
dc.contributor.authorHan, Ju Hee-
dc.contributor.authorYang, Wookjin-
dc.contributor.authorKim, Chi Kyung-
dc.contributor.authorKim, Jaeyun-
dc.contributor.authorLee, Seung-Hoon-
dc.date.accessioned2021-09-02T02:43:04Z-
dc.date.available2021-09-02T02:43:04Z-
dc.date.created2021-06-18-
dc.date.issued2018-12-
dc.identifier.issn0039-2499-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/71481-
dc.description.abstractBackground and Purpose-Despite early aneurysm repair and aggressive management for complications, subarachnoid hemorrhage (SAH) results in at least 25% mortality rate and 50% persistent neurological deficit. We investigated whether ceria nanoparticles which have potent antioxidative activities can protect against subarachnoid hemorrhage via attenuating fatal brain injuries. Methods-Uniform, 3 nm, water-dispersed ceria nanoparticles were prepared from short sol-gel reaction of cerium (III) ions with aminocaproic acid in aqueous phase. SAH was induced by endovascular perforation of middle cerebral artery of rats. A single dose of ceria nanoparticles (0.5 mg Ce/kg) or saline control was randomly administered intravenously at an hour post-SAH. Neuronal death, macrophage infiltration, SAH grade, and brain edema were evaluated at 72 hours. Mortality and neurological function were assessed for 14 days. Results-The obtained ceria nanoparticles with high Ce3+ to Ce4+ ratio demonstrated potent antioxidative, cytoprotective, and anti-inflammatory activities in vitro. In rodent SAH models, the severity of hemorrhage was comparable between the ceria nanoparticles- and saline-treated groups. However, ceria nanoparticles significantly reduced neuronal death, macrophage infiltration, and brain edema after SAH. Ceria nanoparticles successfully improved survival rates (88.2% in the ceria nanoparticles group versus 21.1% in the control group; P<0.001) and neurological outcomes (modified Garcia score: 12.1 +/- 0.5 in the ceria nanoparticles group versus 4.4 +/- 0.5 in the control group; P<0.001) of the animals with SAH. Conclusions-Ceria nanoparticles, totally synthesized in aqueous phase using aminocaproic acid, demonstrated promising results against SAH via potent antioxidative, neuroprotective and anti-inflammatory activities. Given the obvious limitations of current therapies for SAH, ceria nanoparticles can be a potential therapeutic agent which might result in a paradigm shift in SAH treatment. Visual Overview-An online visual overview is available for this article.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherLIPPINCOTT WILLIAMS & WILKINS-
dc.subjectEARLY BRAIN-INJURY-
dc.subjectSUPEROXIDE-DISMUTASE-
dc.subjectBLOOD-FLOW-
dc.subjectDEATH-
dc.subjectINHIBITION-
dc.subjectMECHANISMS-
dc.subjectNECROSIS-
dc.subjectSTRESS-
dc.subjectMODEL-
dc.titleCeria Nanoparticles Synthesized With Aminocaproic Acid for the Treatment of Subarachnoid Hemorrhage-
dc.typeArticle-
dc.contributor.affiliatedAuthorKim, Chi Kyung-
dc.identifier.doi10.1161/STROKEAHA.118.022631-
dc.identifier.scopusid2-s2.0-85058910010-
dc.identifier.wosid000456427700045-
dc.identifier.bibliographicCitationSTROKE, v.49, no.12, pp.3030 - 3038-
dc.relation.isPartOfSTROKE-
dc.citation.titleSTROKE-
dc.citation.volume49-
dc.citation.number12-
dc.citation.startPage3030-
dc.citation.endPage3038-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalResearchAreaCardiovascular System & Cardiology-
dc.relation.journalWebOfScienceCategoryClinical Neurology-
dc.relation.journalWebOfScienceCategoryPeripheral Vascular Disease-
dc.subject.keywordPlusEARLY BRAIN-INJURY-
dc.subject.keywordPlusSUPEROXIDE-DISMUTASE-
dc.subject.keywordPlusBLOOD-FLOW-
dc.subject.keywordPlusDEATH-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordPlusMECHANISMS-
dc.subject.keywordPlusNECROSIS-
dc.subject.keywordPlusSTRESS-
dc.subject.keywordPlusMODEL-
dc.subject.keywordAuthornanomedicine-
dc.subject.keywordAuthorneuroprotective agents-
dc.subject.keywordAuthorreactive oxygen species-
dc.subject.keywordAuthorstroke-
dc.subject.keywordAuthorsubarachnoid hemorrhage-
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